Ectodermal Dysplasia 11b, Hypohidrotic/hair/tooth Type, Autosomal Recessive (ECTD11B)

Alias:
Ectd11b
Ectodermal Dysplasia 11b
Hed
Eda
Dysplasia, Ectodermal, Type 11b, Hypohidrotic/hair/tooth, Autosomal Recessive
Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive
Ectodermal Dysplasia Hypohidrotic Autosomal Recessive
Ectodermal Dysplasia, Hypohidrotic
Ectodermal Dysplasia, Anhidrotic
Ectodermal Dysplasia Anhidrotic
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Ectodermal Dysplasia 11b, Hypohidrotic/hair/tooth Type, Autosomal Recessive, also known as ectd11b, is related to ectodermal dysplasia 11a, hypohidrotic/hair/tooth type, autosomal dominant and pompholyx, and has symptoms including spontaneous, recurrent epistaxis An important gene associated with Ectodermal Dysplasia 11b, Hypohidrotic/hair/tooth Type, Autosomal Recessive is EDARADD (EDAR Associated Via Death Domain), and among its related pathways/superpathways are Cytokine Signaling in Immune system and TNF Superfamily - Human Ligand-Receptor Interactions and their Associated Functions. Affiliated tissues include skin, and related phenotypes are ectodermal dysplasia and absent nipple
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
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5
42
10

Medical Symptom

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Gene & Mutation

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References Literature

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